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Structure of 17193-39-4
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This chiral building block features a (S)-configured methyl ester and a cyclohexyl-substituted alpha-carbon, delivering high enantioselectivity in asymmetric synthesis. The hydrochloride salt enhances solubility and stability under standard handling conditions, facilitating integration into peptide and pharmaceutical intermediates.
(S)-Methyl 2-amino-3-cyclohexylpropanoate hydrochloride serves as a chiral building block for the synthesis of bioactive molecules, leveraging its well-defined stereochemistry and amine functionality. The cyclohexyl group provides conformational rigidity beneficial in medicinal chemistry applications. This compound facilitates efficient peptide coupling and is compatible with standard protecting group strategies, enabling straightforward incorporation into complex scaffolds. Its bench-stable hydrochloride salt form ensures ease of handling and purification.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: